File:Inheritance pattern in Huntington's Disease.jpeg
Inheritance_pattern_in_Huntington's_Disease.jpeg (531 × 284 pixels, file size: 15 KB, MIME type: image/jpeg)
Huntington's disease is an autosomal dominant disorder. If one parent is affected, the child has a 50% chance of inheriting the mutation on the huntingtin gene on their 4th chromosome.
mHTT: Mutant huntingtin
Red squares: HD affected offspring
Illustration by: z3290270
Inspiration: Yale Madical group - Yale School of Medicine [1]
Reference
http://www.yalemedicalgroup.org/stw/Page.asp?PageID=STW025754
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Assessment
+ Figure meets student drawn criteria for project. + Copyright, citation and student disclaimer included. + Figure legend includes explanation for peer teaching component. - Figure design with black background made this picture a little difficult to read details.
- Note - This image was originally uploaded as part of a student project and may contain inaccuracies in either description or acknowledgements. Students have been advised in writing concerning the reuse of content and may accidentally have misunderstood the original terms of use. If image reuse on this non-commercial educational site infringes your existing copyright, please contact the site editor for immediate removal.
Cite this page: Hill, M.A. (2024, April 25) Embryology Inheritance pattern in Huntington's Disease.jpeg. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/File:Inheritance_pattern_in_Huntington%27s_Disease.jpeg
- © Dr Mark Hill 2024, UNSW Embryology ISBN: 978 0 7334 2609 4 - UNSW CRICOS Provider Code No. 00098G
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Date/Time | Thumbnail | Dimensions | User | Comment | |
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current | 12:24, 22 September 2011 | 531 × 284 (15 KB) | Z3290270 (talk | contribs) | Huntington's disease is an autosomal dominant disorder. If one parent is affected, the child has a 50% chance of inheriting the mutation on the huntingtin gene on their 4th chromosome. Illustration by: z3290270 Inspiration: Yale Madical group - Yale Sc |
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